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Structure paper

TitleStructural basis of mutant-selectivity and drug-resistance related to CO-1686.
Journal, issue, pagesOncotarget, Vol. 8, Page 53508-53517, Year 2017
Publish dateMar 28, 2017 (structure data deposition date)
AuthorsYan, X.E. / Zhu, S.J. / Liang, L. / Zhao, P. / Choi, H.G. / Yun, C.H.
External linksOncotarget / PubMed:28881827
MethodsX-ray diffraction
Resolution2.346 - 2.7 Å
Structure data

PDB-5xdk:
Crystal structure of EGFR 696-1022 T790M in complex with CO-1686
Method: X-RAY DIFFRACTION / Resolution: 2.346 Å

PDB-5xdl:
Crystal structure of EGFR 696-1022 L858R in complex with CO-1686
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

Chemicals

ChemComp-8JC:
N-[3-[[2-[[4-(4-ethanoylpiperazin-1-yl)-2-methoxy-phenyl]amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]phenyl]prop-2-enamide / medication, inhibitor*YM

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / EGFR / T790M / inhibitor / L858R

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